Ethnic fracture is a rare condition that affects the child before birth. It occurs at an early stage of pregnancy when the diaphragm fails for the child, which is the muscle that separates the breast from the abdomen, in the closure as it should. It leaves a hole in the diaphragm, and this hole is called a rupture. This fraction in the diaphragm muscle causes an opening between the abdomen and chest. The intestines, stomach, liver and other abdominal organs can cross through the hole to the baby’s chest. And when the intestines enter the breast, it does not form the natural ligaments that stabilize it in the abdomen (bad turn). It can revolve around itself, leading to the cutting of blood supply from it (the infettel). In addition, the lung is on the side of the diaphragm with the rupture small in size, and the growth of both lungs is affected, so the airbags (the air fiber) do not develop within the lungs as it should. It causes blood flow problems and increased pressure in the blood vessels in the lung. High blood pressure in the lungs should make the child’s breathing difficult after birth. Some babies may also have problems with heart growth. Ethnic fracture treatment depends on the time of discovering its condition and its severity and whether there are problems in the heart or not. Symptoms vary the intensity of congenital hijab -breaking. It can be simple and the limited consequences on the child, if any, leave, or it can be more dangerous and affect the ability to transfer oxygen to the rest of the body. Children born with congenital hijab -break can be infected with the following: Serious breathing problems due to the small size of the lungs and their lack of proper (lung weaving). A type of high blood pressure affects the veins in the lungs and the right side of the heart (pulmonary hypertension). Problems associated with heart growth. Damage to the intestines, stomach, liver and other abdominal organs as it rushes to the chest cavity through rupture. In most cases, the causes are not known as the cause of congenital rupture. In some cases, congenital hijab -break may be associated with a genetic disorder or random genetic changes called mutations. In these cases, the child can be born with more problems, such as heart problems, eyes, arms, legs, stomach and intestines. Complications include complications that can occur with congenital rupture: lung problems. Stomach, bowel and liver problems. Heart disease. Repeated infectional cases. Hearing loss. Changes in the shape of the chest and the curvature of the spine. Esophageal denying reflux, which is the return of stomach acid to the esophagus connecting the mouth to the stomach. Problems of growth and weight gain. Developmental delays and learning difficulties. Other problems that exist from birth. Treatment depends on the treatment of congenital Hujabi -break, at the time of discovering the satisfactory condition and its severity. The healthcare team will help determine the best option for parents and children. The preparation of care, the mother health team follows carefully before the child’s birth. Ultrasound and other tests are usually undergoing the health and growth of the child. The new treatment for serious congenital rupture is called the study that is currently a bronchoscopy of the fetus (feto). This operation is performed for the child during pregnancy. This operation aims to motivate my child’s lungs to grow as much as possible. The bronchial closure is performed by the inner theorizing of the fetus by two procedures: the first procedure. The first procedure takes place early in the last few months (third third) of pregnancy. The surgeon makes a small incision in the abdomen and uterus. It introduces a special tube with a camera at the end, called the inner endoscope of the fetus, through the child’s mouth to the coercion (the trachea). A small balloon is placed in the child’s trachy, then this balloon is blown. The natural uterine fluid flows during pregnancy, called the fluid, in the lungs of the child and outside and of them through the mouth. Balloon blows the fluid fluid into my child’s lungs. The liquid helps to expand the lungs to motivate them to grow. The second procedure. After about four to six weeks, the mother will undergo the second procedure. The balloon is removed so that the child is ready to inhale the air in the lungs after birth. A special method of childbirth can be used if labor begins before the balloon is removed and the balloon is not possible to remove the internal laparoscope. This method is called exit treatment during childbirth. The birth is performed by a caesarean section with placenta support. This means that the child still gets oxygen via the placenta before cutting the umbilical cord. The highest support continues until the balloon is extracted and a breathing tube is placed, allowing the device to take over the breathing process. The bronchial closure of the inner theoscopy of the fetus may not be the right choice for all cases. There is nothing to guarantee the results of the operation. The healthcare team assesses the mother’s condition and the condition of the fetus to see if it is eligible to undergo this operation. The mother should talk to the team about the benefits and possible complications for her and the child. During childbirth, the mother can usually bear a normal or caesarean section. And you will decide with the doctor the best way for her. Postpartum Care will help the healthcare team after birth, plan for treatment that meets the child’s needs. The child is likely to receive care in the intensive care unit for newborns. The condition of the child may need a breathing tube for him. This tube is connected to a device that helps the child breathe. It gives the lungs and heart the time for growth and development. Children with lifestyle pulmonary problems may require a treatment called membrane oxidants outside the body. This treatment is also called life support outside the body. The membrane box outside the body performs the functions of the child’s heart and lungs, giving these organs the opportunity to rest and restore. The child’s need for breathing support depends on the response to treatment and other factors. Most children with congenital hijab -break undergo surgery to lock the hole in the diaphragm. The date of this operation is determined based on the health of the child and other factors. Inspection care usually contains x -ray photography to ensure the safety of recovery. After leaving the hospital, the child may need extra support. This may include supplementary oxygen. The oxygen is connected to a thin plastic tube equipped with the edges of the nose, or a thin tube connected to a mask placed on the nose and mouth. The need can also ask nutritional support to grow and develop. Medicines can be prescribed for cases associated with congenital rupture, such as acid reflux or pulmonary hypertension. *This content of “Mayo Clinic” also reads:
Ethnic hijab rupture .. causes, symptoms and treatment
